Canonical Allele Identifier: CA405427871

Gene: KMT2B

Linked Data

• MyVariant Identifiers: chr19:g.36223787A>G (hg19) ; chr19:g.35732886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35732886A>G , CM000681.2:g.35732886A>G	GRCh38
NC_000019.9:g.36223787A>G , CM000681.1:g.36223787A>G	GRCh37
NC_000019.8:g.40915627A>G	NCBI36
NG_052906.1:g.19868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592092.2:n.643A>G
ENST00000673918.2:c.6271A>G	ENSP00000501283.1:p.Ile2091Val
ENST00000674114.2:c.3878A>G	ENSP00000501039.2:n.3878A>G
ENST00000684977.1:c.1555A>G	ENSP00000509384.1:p.Ile519Val
ENST00000689544.1:n.1490A>G
ENST00000691421.1:c.1558A>G	ENSP00000508674.1:p.Ile520Val
ENST00000691855.1:c.5879A>G
ENST00000692961.1:c.6337A>G	ENSP00000509289.1:p.Ile2113Val
ENST00000693677.1:c.704+557A>G	ENSP00000509779.1:n.704+557A>G
ENST00000420124.4:c.6337A>G MANE Select	ENSP00000398837.2:p.Ile2113Val
ENST00000673918.1:c.6271A>G	ENSP00000501283.1:p.Ile2091Val
ENST00000674114.1:c.3659A>G
ENST00000420124.2:c.6337A>G	ENSP00000398837.1:p.Ile2113Val
NM_014727.2:c.6337A>G	NP_055542.1:p.Ile2113Val
XM_011527561.1:c.6271A>G	XP_011525863.1:p.Ile2091Val
XM_011527562.1:c.6337A>G	XP_011525864.1:p.Ile2113Val
XM_011527563.1:c.6061A>G	XP_011525865.1:p.Ile2021Val
XM_011527561.2:c.5773A>G	XP_011525863.2:p.Ile1925Val
XM_011527562.2:c.6337A>G	XP_011525864.1:p.Ile2113Val
XM_017027544.1:c.6337A>G	XP_016883033.1:p.Ile2113Val
XM_017027545.1:c.5773A>G	XP_016883034.1:p.Ile1925Val
XM_017027546.1:c.3301A>G	XP_016883035.1:p.Ile1101Val
NM_014727.3:c.6337A>G MANE Select	NP_055542.1:p.Ile2113Val